Synthetic study of tetramethyljulolidine - a key intermediate toward the synthesis of the red dopant DCJTB for OLED applications
| dc.citation.epage | 147 | en_US |
| dc.citation.issue | 1 | en_US |
| dc.citation.spage | 145 | en_US |
| dc.citation.volume | 44 | en_US |
| dc.citation.woscount | 18 | |
| dc.contributor.author | Balaganesan, B | en_US |
| dc.contributor.author | Wen, SW | en_US |
| dc.contributor.author | Chen, CH | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | 友訊交大聯合研發中心 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.contributor.department | D Link NCTU Joint Res Ctr | en_US |
| dc.date.accessioned | 2014-12-08T15:41:27Z | |
| dc.date.available | 2014-12-08T15:41:27Z | |
| dc.date.issued | 2003-01-01 | en_US |
| dc.description.abstract | The formation and characterization of a novel chiral sulfonic acid derivative obtained during the synthesis of 1,1,7,7-tetramethyljulolidine (TMJ), a key intermediate towards the red dopant 4-(dicyanomethylene)-2-t-butyl-6-(1,1,7,7-tetramethyljutolidyl-9-enyl)-4H-pyran (DCJTB) used for organic electroluminescent devices, upon bis-annulation of NN-bis(4-methyl-2-butenyl)aniline is described. (C) 2002 Elsevier Science Ltd. All rights reserved. | en_US |
| dc.identifier.doi | 10.1016/S0040-4039(02)02506-6 | en_US |
| dc.identifier.issn | 0040-4039 | en_US |
| dc.identifier.journal | TETRAHEDRON LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/S0040-4039(02)02506-6 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/28194 | |
| dc.identifier.wosnumber | WOS:000180094700035 | |
| dc.language.iso | en_US | en_US |
| dc.title | Synthetic study of tetramethyljulolidine - a key intermediate toward the synthesis of the red dopant DCJTB for OLED applications | en_US |
| dc.type | Article | en_US |